3-Methyl-2H-indazole

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Reagent Code: #213103
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CAS Number 50407-19-7

science Other reagents with same CAS 50407-19-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 132.16 g/mol
Formula C₈H₈N₂
badge Registry Numbers
MDL Number MFCD00601361
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in synthesizing biologically active molecules. It is particularly valuable in the creation of kinase inhibitors, which are important in the treatment of cancers and inflammatory diseases. Its structure allows for easy modification, making it useful in optimizing drug candidates for improved potency and selectivity. Additionally, it has been explored in the development of central nervous system agents due to its ability to cross the blood-brain barrier. In agrochemical research, derivatives of this compound contribute to the design of new pesticides with enhanced activity and environmental safety. Its versatility in forming stable complexes with metal ions also supports its use in catalysis during synthetic processes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,630.00
inventory 5g
10-20 days ฿5,710.00
inventory 25g
10-20 days ฿22,320.00

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3-Methyl-2H-indazole
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in synthesizing biologically active molecules. It is particularly valuable in the creation of kinase inhibitors, which are important in the treatment of cancers and inflammatory diseases. Its structure allows for easy modification, making it useful in optimizing drug candidates for improved potency and selectivity. Additionally, it has been explored in the development of central nervous system agents due to its ability to cross the blood-brain barrier. In agrochemical research, derivatives of this compound contribute to the design of new pesticides with enhanced activity and environmental safety. Its versatility in forming stable complexes with metal ions also supports its use in catalysis during synthetic processes.
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